Abstract

BackgroundSugarcane is an important sugar crop contributing up to about 80% of the world sugar production. Efforts to characterize the genes involved in sugar metabolism at the molecular level are growing since increasing sugar content is a major goal in the breeding of new sugarcane varieties. Fructokinases (FRK) are the main fructose phosphorylating enzymes with high substrate specificity and affinity.ResultsIn this study, by combining comparative genomics approaches with BAC resources, seven fructokinase genes were identified in S. spontaneum. Phylogenetic analysis based on representative monocotyledon and dicotyledon plant species suggested that the FRK gene family is ancient and its evolutionary history can be traced in duplicated descending order: SsFRK4, SsFRK6/SsFRK7,SsFRK5, SsFRK3 and SsFRK1/SsFRK2. Among the close orthologs, the number and position of exons in FRKs were conserved; in contrast, the size of introns varied among the paralogous FRKs in Saccharum. Genomic constraints were analyzed within the gene alleles and between S. spontaneum and Sorghum bicolor, and gene expression analysis was performed under drought stress and with exogenous applications of plant hormones. FRK1, which was under strong functional constraint selection, was conserved among the gene allelic haplotypes, and displayed dominant expression levels among the gene families in the control conditions, suggesting that FRK1 plays a major role in the phosphorylation of fructose. FRK3 and FRK5 were dramatically induced under drought stress, and FRK5 was also found to increase its expression levels in the mature stage of Saccharum. Similarly, FRK3 and FRK5 were induced in response to drought stress in Saccharum. FRK2 and FRK7 displayed lower expression levels than the other FRK family members; FRK2 was under strong genomic selection constraints whereas FRK7 was under neutral selection. FRK7 may have become functionally redundant in Saccharum through pseudogenization. FRK4 and FRK6 shared the most similar expression pattern: FRK4 was revealed to have higher expression levels in mature tissues than in premature tissues of Saccharum, and FRK6 presented a slight increase under drought stress.ConclusionsOur study presents a comprehensive genomic study of the entire FRK gene family in Saccharum, providing the foundations for approaches to characterize the molecular mechanism regulated by the SsFRK family in sugarcane.

Highlights

  • Sugarcane is an important sugar crop contributing up to about 80% of the world sugar production

  • FRK3 and FRK5 were both dramatically induced by Polyethylene glycol (PEG) treatment, the three FRKs including FRK1, FRK3 and FRK5 were predominant expression under drought stress (Fig. 7a). These results revealed that FRK3 and FRK5 played a main role in response to drought stress in Saccharum, and indicated that the phosphorylation of Glc to G6P and Fru to fructose 6-phosphate (F6P) were involved in response to drought stress in Saccharum

  • In this study, by combining comparative genomics approaches with Bacterial artificial chromosomes (BACs), we identified the fructokinase gene family consisting of seven members in S. spontaneum

Read more

Summary

Introduction

Sugarcane is an important sugar crop contributing up to about 80% of the world sugar production. Efforts to characterize the genes involved in sugar metabolism at the molecular level are growing since increasing sugar content is a major goal in the breeding of new sugarcane varieties. Sugarcane (Saccharum spp.) is a large, perennial, tropical or subtropical crop. It is one of the world’s most produced crops (FAOSTAT, 2015) contributing about 80% of the world sugar production (FAOSTAT, 2010). Sorghum is the closest diploid species of Saccharum, and has a genome size about 760 Mb which has been sequenced [9]. It is possible to identify sugarcane genes by combining the BAC sequences and the available sorghum genome data

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call